Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam9 |
T |
A |
8: 25,452,938 (GRCm39) |
R790* |
probably null |
Het |
Adamts13 |
C |
A |
2: 26,880,624 (GRCm39) |
P736T |
probably benign |
Het |
Aldh3b2 |
T |
A |
19: 4,028,859 (GRCm39) |
F176L |
possibly damaging |
Het |
Aldoart2 |
A |
G |
12: 55,612,696 (GRCm39) |
E207G |
probably benign |
Het |
Arid4b |
A |
T |
13: 14,361,535 (GRCm39) |
E753D |
probably benign |
Het |
Cd160 |
T |
A |
3: 96,709,662 (GRCm39) |
T158S |
probably benign |
Het |
Cd209g |
T |
A |
8: 4,185,195 (GRCm39) |
M1K |
probably null |
Het |
Chrm4 |
A |
G |
2: 91,758,204 (GRCm39) |
Y204C |
probably damaging |
Het |
Cyld |
T |
A |
8: 89,456,346 (GRCm39) |
N465K |
probably benign |
Het |
Dchs1 |
A |
T |
7: 105,405,128 (GRCm39) |
H2471Q |
possibly damaging |
Het |
Dchs1 |
A |
G |
7: 105,411,189 (GRCm39) |
V1612A |
probably damaging |
Het |
Ddx24 |
A |
G |
12: 103,382,477 (GRCm39) |
V702A |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 31,003,127 (GRCm39) |
T3609A |
possibly damaging |
Het |
Dock5 |
A |
T |
14: 68,040,426 (GRCm39) |
|
probably null |
Het |
Dpy19l2 |
C |
T |
9: 24,591,988 (GRCm39) |
R205H |
probably damaging |
Het |
Eif3a |
A |
T |
19: 60,762,363 (GRCm39) |
D473E |
probably damaging |
Het |
Elapor1 |
G |
T |
3: 108,399,398 (GRCm39) |
T64K |
probably benign |
Het |
Elobl |
T |
C |
11: 88,855,796 (GRCm39) |
E89G |
possibly damaging |
Het |
Fam186a |
A |
T |
15: 99,841,351 (GRCm39) |
I1631N |
possibly damaging |
Het |
Fbn2 |
C |
T |
18: 58,159,496 (GRCm39) |
W2411* |
probably null |
Het |
Fbxl17 |
A |
G |
17: 63,367,360 (GRCm39) |
I671T |
probably damaging |
Het |
Glul |
C |
T |
1: 153,782,868 (GRCm39) |
T193I |
possibly damaging |
Het |
H4c16 |
A |
G |
6: 136,781,124 (GRCm39) |
M85T |
probably benign |
Het |
Hr |
A |
G |
14: 70,795,381 (GRCm39) |
T309A |
probably benign |
Het |
Ighg3 |
A |
G |
12: 113,324,158 (GRCm39) |
S110P |
probably benign |
Het |
Llgl2 |
A |
G |
11: 115,737,755 (GRCm39) |
E180G |
possibly damaging |
Het |
Mat2b |
A |
T |
11: 40,576,092 (GRCm39) |
L112Q |
probably damaging |
Het |
Mcoln2 |
T |
C |
3: 145,896,169 (GRCm39) |
M497T |
probably damaging |
Het |
Mmp24 |
C |
A |
2: 155,649,481 (GRCm39) |
Y299* |
probably null |
Het |
Mtor |
T |
C |
4: 148,610,260 (GRCm39) |
|
probably null |
Het |
Olig2 |
C |
A |
16: 91,023,299 (GRCm39) |
D4E |
probably damaging |
Het |
Or10ag2 |
A |
T |
2: 87,248,889 (GRCm39) |
I164L |
probably benign |
Het |
Pard3 |
T |
C |
8: 128,142,077 (GRCm39) |
S878P |
probably damaging |
Het |
Pcgf5 |
C |
T |
19: 36,417,483 (GRCm39) |
P137L |
probably damaging |
Het |
Pck1 |
A |
G |
2: 172,997,071 (GRCm39) |
N238D |
probably damaging |
Het |
Pstpip1 |
T |
C |
9: 56,035,064 (GRCm39) |
S346P |
probably benign |
Het |
Qsox2 |
G |
A |
2: 26,114,897 (GRCm39) |
H40Y |
possibly damaging |
Het |
Rbpj |
T |
C |
5: 53,799,479 (GRCm39) |
I129T |
probably damaging |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Saal1 |
G |
A |
7: 46,360,031 (GRCm39) |
P9L |
probably benign |
Het |
Sema3c |
A |
G |
5: 17,932,362 (GRCm39) |
I622V |
probably benign |
Het |
Sigirr |
C |
T |
7: 140,671,785 (GRCm39) |
V333M |
probably benign |
Het |
Sort1 |
T |
C |
3: 108,246,183 (GRCm39) |
S387P |
probably damaging |
Het |
Spata31h1 |
A |
C |
10: 82,132,520 (GRCm39) |
Y163* |
probably null |
Het |
Spta1 |
T |
A |
1: 174,014,797 (GRCm39) |
S426T |
probably benign |
Het |
Stag3 |
G |
A |
5: 138,281,404 (GRCm39) |
S124N |
probably damaging |
Het |
Stard10 |
A |
G |
7: 100,993,176 (GRCm39) |
Y244C |
probably damaging |
Het |
Tcea3 |
T |
A |
4: 135,995,440 (GRCm39) |
I261N |
probably damaging |
Het |
Tdrd1 |
A |
G |
19: 56,832,267 (GRCm39) |
K395E |
probably damaging |
Het |
Tenm2 |
T |
A |
11: 35,918,048 (GRCm39) |
D1905V |
probably benign |
Het |
Trim12c |
T |
C |
7: 103,990,037 (GRCm39) |
Y480C |
unknown |
Het |
Trip11 |
A |
G |
12: 101,849,741 (GRCm39) |
V1441A |
probably damaging |
Het |
Ttc21a |
G |
A |
9: 119,795,392 (GRCm39) |
R1107Q |
probably benign |
Het |
Wdr41 |
A |
G |
13: 95,153,838 (GRCm39) |
I296V |
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,345,260 (GRCm39) |
V1213E |
possibly damaging |
Het |
Zfp37 |
T |
C |
4: 62,109,553 (GRCm39) |
N545D |
possibly damaging |
Het |
|
Other mutations in Grm7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01729:Grm7
|
APN |
6 |
111,223,145 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02058:Grm7
|
APN |
6 |
111,335,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Grm7
|
APN |
6 |
111,335,919 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Grm7
|
APN |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03074:Grm7
|
APN |
6 |
111,472,604 (GRCm39) |
splice site |
probably null |
|
IGL03185:Grm7
|
APN |
6 |
110,623,183 (GRCm39) |
missense |
possibly damaging |
0.84 |
Appropriated
|
UTSW |
6 |
111,472,642 (GRCm39) |
missense |
possibly damaging |
0.64 |
Consumed
|
UTSW |
6 |
111,335,836 (GRCm39) |
missense |
probably damaging |
1.00 |
Devoured
|
UTSW |
6 |
111,335,785 (GRCm39) |
missense |
probably damaging |
1.00 |
Ravaged
|
UTSW |
6 |
111,335,874 (GRCm39) |
missense |
probably damaging |
1.00 |
shaky
|
UTSW |
6 |
111,472,752 (GRCm39) |
nonsense |
probably null |
|
PIT4651001:Grm7
|
UTSW |
6 |
110,623,050 (GRCm39) |
missense |
probably benign |
|
R0539:Grm7
|
UTSW |
6 |
111,336,055 (GRCm39) |
splice site |
probably benign |
|
R0622:Grm7
|
UTSW |
6 |
111,335,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1356:Grm7
|
UTSW |
6 |
111,335,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Grm7
|
UTSW |
6 |
111,472,752 (GRCm39) |
nonsense |
probably null |
|
R1823:Grm7
|
UTSW |
6 |
111,184,730 (GRCm39) |
missense |
probably benign |
0.17 |
R1864:Grm7
|
UTSW |
6 |
111,057,384 (GRCm39) |
missense |
probably benign |
0.03 |
R1894:Grm7
|
UTSW |
6 |
111,335,568 (GRCm39) |
missense |
probably benign |
|
R1987:Grm7
|
UTSW |
6 |
110,891,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Grm7
|
UTSW |
6 |
111,184,769 (GRCm39) |
missense |
probably benign |
0.13 |
R2138:Grm7
|
UTSW |
6 |
110,623,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Grm7
|
UTSW |
6 |
111,335,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2289:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2296:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2339:Grm7
|
UTSW |
6 |
111,472,642 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2847:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2849:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2879:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2921:Grm7
|
UTSW |
6 |
111,472,866 (GRCm39) |
splice site |
probably null |
|
R2923:Grm7
|
UTSW |
6 |
111,472,866 (GRCm39) |
splice site |
probably null |
|
R3014:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3015:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3703:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4009:Grm7
|
UTSW |
6 |
111,472,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Grm7
|
UTSW |
6 |
110,891,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R4131:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4132:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4161:Grm7
|
UTSW |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R4329:Grm7
|
UTSW |
6 |
110,891,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4357:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4359:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Grm7
|
UTSW |
6 |
111,223,335 (GRCm39) |
missense |
probably benign |
0.05 |
R4379:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4380:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Grm7
|
UTSW |
6 |
111,335,265 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4518:Grm7
|
UTSW |
6 |
110,891,507 (GRCm39) |
splice site |
probably null |
|
R4647:Grm7
|
UTSW |
6 |
110,891,344 (GRCm39) |
nonsense |
probably null |
|
R4714:Grm7
|
UTSW |
6 |
111,057,383 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4775:Grm7
|
UTSW |
6 |
110,891,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Grm7
|
UTSW |
6 |
111,335,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:Grm7
|
UTSW |
6 |
111,057,404 (GRCm39) |
missense |
probably damaging |
0.99 |
R5062:Grm7
|
UTSW |
6 |
110,623,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Grm7
|
UTSW |
6 |
111,335,182 (GRCm39) |
missense |
probably benign |
0.01 |
R5431:Grm7
|
UTSW |
6 |
111,335,387 (GRCm39) |
missense |
probably benign |
|
R6026:Grm7
|
UTSW |
6 |
111,478,500 (GRCm39) |
nonsense |
probably null |
|
R6174:Grm7
|
UTSW |
6 |
111,223,258 (GRCm39) |
missense |
probably benign |
|
R6305:Grm7
|
UTSW |
6 |
111,335,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Grm7
|
UTSW |
6 |
111,335,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R6440:Grm7
|
UTSW |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R6519:Grm7
|
UTSW |
6 |
111,184,713 (GRCm39) |
missense |
probably benign |
0.00 |
R6531:Grm7
|
UTSW |
6 |
111,335,386 (GRCm39) |
missense |
probably benign |
0.29 |
R6888:Grm7
|
UTSW |
6 |
111,335,314 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6949:Grm7
|
UTSW |
6 |
111,472,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Grm7
|
UTSW |
6 |
110,623,265 (GRCm39) |
missense |
probably benign |
0.03 |
R6989:Grm7
|
UTSW |
6 |
111,184,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:Grm7
|
UTSW |
6 |
111,335,113 (GRCm39) |
missense |
probably benign |
0.04 |
R7203:Grm7
|
UTSW |
6 |
111,335,530 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7208:Grm7
|
UTSW |
6 |
111,335,530 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7217:Grm7
|
UTSW |
6 |
111,335,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Grm7
|
UTSW |
6 |
110,623,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R7297:Grm7
|
UTSW |
6 |
110,622,974 (GRCm39) |
missense |
probably benign |
0.16 |
R7470:Grm7
|
UTSW |
6 |
111,478,476 (GRCm39) |
missense |
|
|
R7567:Grm7
|
UTSW |
6 |
111,335,722 (GRCm39) |
missense |
probably damaging |
0.96 |
R7806:Grm7
|
UTSW |
6 |
111,223,314 (GRCm39) |
nonsense |
probably null |
|
R8018:Grm7
|
UTSW |
6 |
111,184,737 (GRCm39) |
missense |
probably benign |
0.01 |
R8409:Grm7
|
UTSW |
6 |
110,891,297 (GRCm39) |
missense |
probably benign |
0.02 |
R8420:Grm7
|
UTSW |
6 |
111,057,315 (GRCm39) |
missense |
probably benign |
|
R8523:Grm7
|
UTSW |
6 |
111,223,280 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8816:Grm7
|
UTSW |
6 |
111,230,966 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8958:Grm7
|
UTSW |
6 |
111,472,783 (GRCm39) |
missense |
probably damaging |
0.96 |
R9135:Grm7
|
UTSW |
6 |
111,472,729 (GRCm39) |
missense |
probably benign |
0.39 |
R9207:Grm7
|
UTSW |
6 |
111,335,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Grm7
|
UTSW |
6 |
110,622,869 (GRCm39) |
missense |
probably benign |
0.01 |
R9438:Grm7
|
UTSW |
6 |
111,231,077 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9448:Grm7
|
UTSW |
6 |
111,335,193 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Grm7
|
UTSW |
6 |
111,335,451 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Grm7
|
UTSW |
6 |
111,335,110 (GRCm39) |
missense |
probably benign |
0.01 |
|